A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614554



Internal ID20987625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87865927..87869342hg38UCSC Ensembl
chr7:87495242..87498657hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg383416
hg193416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161883
Samples
Known GenesSLC25A40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614554
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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